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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C1335512 | Prostate Lymphoma | OPCML | 4978 | opioid binding protein/cell adhesion molecule like | Q14982 |
| C0278878 | Adult Glioblastoma | OPCML | 4978 | opioid binding protein/cell adhesion molecule like | Q14982 |
| C0376358 | Malignant neoplasm of prostate | OPCML | 4978 | opioid binding protein/cell adhesion molecule like | Q14982 |
| C3542025 | AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE | OPCML | 4978 | opioid binding protein/cell adhesion molecule like | Q14982 |
| C0038356 | Stomach Neoplasms | OPCML | 4978 | opioid binding protein/cell adhesion molecule like | Q14982 |
| C0004997 | Benign Ovarian Neoplasm | OPCML | 4978 | opioid binding protein/cell adhesion molecule like | Q14982 |
| C0004096 | Asthma | ORMDL1 | 94101 | ORMDL sphingolipid biosynthesis regulator 1 | Q9P0S3 |
| C0004096 | Asthma | ORMDL2 | 29095 | ORMDL sphingolipid biosynthesis regulator 2 | Q53FV1 |
| C0025202 | melanoma | OS9 | 10956 | OS9 endoplasmic reticulum lectin | Q13438 |
| C4551686 | Malignant neoplasm of soft tissue | OS9 | 10956 | OS9 endoplasmic reticulum lectin | Q13438 |
| C1261473 | Sarcoma | OS9 | 10956 | OS9 endoplasmic reticulum lectin | Q13438 |
| C0003873 | Rheumatoid Arthritis | OS9 | 10956 | OS9 endoplasmic reticulum lectin | Q13438 |
| C1846896 | Deafness, Autosomal Recessive 22 | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0268237 | Cytochrome-c Oxidase Deficiency | OTOA | 146183 | otoancorin | Q7RTW8 |
| C1846647 | DEAFNESS, AUTOSOMAL RECESSIVE (disorder) | OTOA | 146183 | otoancorin | Q7RTW8 |
| C1282975 | von Willebrand Disease, Type 2N | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0018784 | Sensorineural Hearing Loss (disorder) | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0302280 | Adrenogenital Syndrome | OTOA | 146183 | otoancorin | Q7RTW8 |
| C1384666 | hearing impairment | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0452138 | Sensorineural hearing loss, bilateral | OTOA | 146183 | otoancorin | Q7RTW8 |
| C3150275 | COMPLEMENT COMPONENT 2 DEFICIENCY | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0001627 | Congenital adrenal hyperplasia | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0221757 | alpha 1-Antitrypsin Deficiency | OTOA | 146183 | otoancorin | Q7RTW8 |
| C1862941 | Amyotrophic Lateral Sclerosis, Sporadic | OTOG | 340990 | otogelin | Q6ZRI0 |
| C3554163 | DEAFNESS, AUTOSOMAL RECESSIVE 18B | OTOG | 340990 | otogelin | Q6ZRI0 |
